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NCT06911567 · ClinicalTrials.gov registry record · Phase 1
A Study to Assess New Formulations of TEV-56286
A Phase 1 study of Healthy Participants, sponsored by Teva Branded Pharmaceutical Products R&D.
- Completed
- Registry status
- Phase 1
- Development phase
- 47
- Enrollment target
- 1
- Study location
NCT06911567 is a Phase 1 study of Healthy Participants that has completed, run by Teva Branded Pharmaceutical Products R&D. The registered enrollment target is 47 participants, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (28% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06911567, a Phase 1 study of Healthy Participants, has completed, sponsored by Teva Branded Pharmaceutical Products R&D.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 47 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of the study is to assess the relative bioavailability of TEV-56286 test formulations compared to TEV-56286 reference product in healthy adult participants. The secondary objective is to evaluate the safety and tolerability of TEV-56286. The planned duration for each participant is approximately 70 days which includes a 45 day screening period.
Conditions Studied
Interventions
- DRUG TEV-56286 Test
- DRUG TEV-56286 Reference
Study Locations (1)
Florida
- Teva Investigational Site 12141 - Miramar
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 47 participants |
| Start Date | 2025-03-10 |
| Est. Completion | 2025-06-02 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06911567
The ClinicalTrials.gov registry entry for NCT06911567 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (28% lower). The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 167 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions - of which TEV-56286 Test is the first listed.
NCT06911567 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT06911567 about?
NCT06911567 is a clinical study titled "A Study to Assess New Formulations of TEV-56286". The primary objective of the study is to assess the relative bioavailability of TEV-56286 test formulations compared to TEV-56286 reference product in healthy adult participants. The secondary objective is to evaluate the safety and tolerability of TEV-56286. The planned duration for each particip...
What is the current status of trial NCT06911567?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2025-03-10. Estimated completion is 2025-06-02.
What conditions does trial NCT06911567 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT06911567?
The interventions under investigation include: TEV-56286 Test (DRUG), TEV-56286 Reference (DRUG).
Who is sponsoring clinical trial NCT06911567?
This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 167 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06911567 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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